Beschreibung
Data Analyst - (m/f/d)Are you an experienced Data Analyst (m/f/d) looking for a new project? We are currently looking urgently for an experienced Data Analyst with a background in Medical Device or Pharma.
Role
- Support RA Business Lead in development and creation of IT System documentation for new functionality related to Technical Documentation requirements, business improvements and further, requirements to be established under MDR
- Perform User Acceptance Testing of newly implemented IT requirements as assigned
- Create and support Software Life Cycle Development documentation
- Provide regulatory support for Life Cycle Management projects as assigned
- Create and maintain global share point(s) for Regulatory Affairs
- Create redlines on impacted business procedures based on the requirement changes from the IT projects
- Manage data cleansing and comparison, remediation and maintenance of existing Technical File documentation as instructed and assigned
- Coordination of stakeholder management
Required skills
- Broad knowledge in database and data science incl. data management
- Hands-on person: knowing how to work with tables, comparisons, macros
- Strong analytical skills
- Expert in MS office (focus on Excel, share point, power query)
- Experience in IT system documentation
- Understand the Medical device or Pharma environment
- Experienced in Requirements Engineering and User Acceptance Testing
- Familiar with business process creation and creation of training materials
- Comprehensive knowledge in the handling with and of data in PLM and ERP system, preferentially experience in Agile e6, ERP (SAP), Windchill
- Supporting hyper care phase
- Experienced skills in MS Office (Excel, Word, Access) for data analyses and comparisons
- Strong analytical skills
- Proficiency in English written and spoken. German in addition, but not required.
- Knowledge in project management
- Basic understanding of MDR requirements regarding required content of Technical Documentation (focus on ANNEX II of Regulation (EU) , MDR)
- Basic understanding of requirements of current Council Directive 93/42/EEC (MDD)
- University/Bachelors Degree or Equivalent
Further information
- Location: Solothurn, Switzerland
- Start date: asap
- Duration: initially until the end of 2023
Interested?
If you would like to apply for this pharmaceutical project as Data Analyst - (m/f/d), please contact Arlinda Konjuhi via phone or E-Mail for more information. Or you can apply directly by clicking the Apply button.
We are looking forward to your application.
Sthree Switzerland is acting as an Employment Business in relation to this vacancy.